Denatured carob flour (dcf) with a low content of soluble tannins and sugars, meant for human consumption and process to obtain it

ABSTRACT

The present invention provides an improved denatured carob flour, which includes 2 to 15% sugars, 0.2 to 1.5% cyclitols (pinitol), 2 to 10% lignins, 10 to 30% celluloses, 3 to 20% hemicelluloses, 1 to 6% pectins, 25 to 55% condensed tannins, 3 to 9% protein and less than 8% water. The invention further provides a process to obtain a denatured carob flour that includes the following steps: a. cleaning the whole fruit; b. crushing the carob fruits; c. separating the carob seeds and kibbled carob pulp, d. toasting between 130 to 200° C.; e. an extracting process; f. separating; g. milling 90% of particles below 250 pm; h. separating; i. drying below 8%; and j. classifying (sieving).

FIELD OF THE INVENTION

Denatured carob flour and the process to obtain it described in this specification will be applied in industry to develop dietary fiber products rich in condensed tannins for human consumption.

DESCRIPTION OF PRIOR ART

There is considerable interest in developing dietary fiber products rich in polyphenol compounds owing to the known protective role of these substances against cardiovascular disease by reducing hypercholesterolemia and their effects on the efficacy of the intestinal translocation and the prevention of colonic cancer.

Hence, to cite some studies from the literature, polyphenolic compounds present in different concentrations in dietary fiber and in different food compounds have important antioxidant effects (Pulido R, Bravo L, Saura-Calixto F. Antioxidant activity of dietary polyphenols as determined by a modified ferric reducing/antioxidant power assay. J. Agric Food Chem (2000) 48(8): 3396-402), that can be used to prevent and treat certain diseases including cancer (Pool-Zobel B L, Adlercreutz H, Glei M, Liegibel U M, Sittlingon J., Rowland I., Wahala K, Rechkemmer G. Isoflavonoids and lignans have different potentials to modulate oxidative genetic damage in human colon cells). Carcinogenesis (2000) 21(6): 1247-52). Nevertheless, there is only a small amount of condensed tannins in the different dietary fibers and products enriched in these natural polyphenols cannot be used in the chronic treatment of degenerative diseases because at these levels they have a strong astringent and antinutritional effect.

On the other hand, pectins, gums and other similar products, majority components of soluble fibers, although substances produced by their colonic fermentation (e.g. butyrate) have been found to have potentially therapeutic applications, important benefits for the immune system (Perez R. Stevenson f. Jhonson J., Morgan M., Ericson K. Hubbard N. E. Morand L. Ruduch S., Kaztnelson S. Sodium butyrate upregulates Kupffer cells PGE-2 production avid modulates immune function. J. Surg. Res. (1998) 78, 1-6; Lim B. O. Yamada K. Nonaka M. Kuramoto Y., Hung P., Sugano M. Dietary fibres modulate indices of intestinal immune function in rats. J. Nutr. (1997) 127, 663-7.) and in the prevention of colonic cancer in cell culture studies (Sowa Y, Sakai T. Butyrate as a model for “gene-regulating chemoprevention and chemotherapy” biofactors (2000); 12 (1-4): 283-7), in human trials the results are not as clear, probably because they ferment rapidly in the proximal colon and little butyrate arrives at the distal colon, the most common site of neoplasic processes (Perrin P, Pierre F, Patry Y, Champ M, Berreur M, Pardal G, Bornet F, Meflah K, Menanteau J. Only fibers promoting a stable butyrate producing colonic ecosystem decrease the rate of aberrant crypt foci in rats. Gut. (2001) 48(1): 53-61). Nevertheless, mainly because of economic interest in animal production, the delaying effect of tannins on bacterial fermentation in the digestive tract is currently well known. Therefore, in suitable quantities they can regulate and delay the production of butyrate in the final portions of the colon and rectum.

Carob pulp is also rich in cyclitol and pinitol, a product that is transformed into inositol in the organism, a molecule of great interest for cell metabolism control (Bates S H, Jones R B, Bailey C J. Insulin-like effect of pinitol. Br J Pharacol (2000) 130 (8): 1944-48). The object of the present invention is, therefore, to eliminate from the carob pulp a large proportion of its sugars and soluble tannins, but maintaining a significant pinitol contents and to modify its condensed tannins to maintain its beneficial effects (hypolipaemic activity), regulators of intestinal function, antioxidants etc), eliminate its astringent and antinutritional effects and to be able to use in this way the product as a dietary product for human or animal use, as well as a component in pharmaceuticals.

DESCRIPTION OF THE INVENTION

The denatured carob flour with low soluble tannin and sugar contents, described here, has the following composition, depending on the variety of fruit used:

-   Sugars . . . usually 2-15%, typically 3-10% -   Cyclitols (pinitol) . . . usually 0.2-1.5%; typically 0.3-1% -   Lignins . . . usually 2-10% ; typically 2-7% -   Celluloses . . . usually 10-30% ; typically 15-28% -   Hemicelluloses . . . usually 3-20% ; typically 3-9% -   Pectins . . . usually 1-6%; typically 2-5% -   Condensed tannins . . . usually 25-55%; typically 30-48% -   Protein . . . usually 3-9%; typically 4-8% -   Water contents less than . . . usually below 8%; typically below 6%

All percentages given are weight percentages (wt.-%) if not stated otherwise.

This carob flour is characterized by having an active ingredient with at least 25%, usually 30%, typically 40% of condensed carob tannins denatured thermally with a weight ratio of soluble to insoluble polyphenols less than 0.05 (solubility determined with water at 37° C.). Evaluation of the polyphenol contents has been carried out by first determining the soluble tannin contents in water at 37° C. stirring for 15 minutes; these are determined spectrophotrometrically in this water with the Folin-Ciocalteau reagent (Singleton V. L. Rossi J. A. Colonimetry of total phenolics with phosphomolybdicphosphotungstic acid reagents. Am. J. Enol. Vitic (1965). 16:144-158). The insoluble polyphenols of the residue are determined by treatment with HCl-butanol according to the method of Hagerman and coworkers (Hagerman A. E. Zhao Y. Jonson S. Methods for determination of condensed and hydrolyzable tannins. In F. Shahidi (Ed), Antinutrients and phytochemicals in foods (p. 209-222). ACS symposium Series 662. Washington, DC. American Chemical Society).

In this invention, carob pulp, rich in condensed tannins, formed by polymerization of flavan-3-ol and its gallic esters with a strong astringent effect, are treated with heat (between usually 130 and 200° C., typically 140 and 150° C.) to result in a change of structure of the polyphenols with partial degradation and polymerization and to eliminate astringency and interference with absorption of nutrients in the diet but maintaining most of its positive effects. It can, therefore, be used for human diet and nutrition (as ordinary foods, enriched foods, dietary foods, foods for special medical purposes or dietary supplements), without antinutritional problems, while the effects of these condensed tannins as a sequesterant of cholesterol and bile salts, as antioxidants, laxatives and regulators of intestinal fermentation are maintained. Furthermore applications in animal feed and pet food or in human and animal pharmaceuticals are possible.

The process to obtain the previously described carob flour consists in a series of steps, as follows:

-   -   a. Cleaning the whole fruit: Cleaning includes e.g dry (e.g.         mechanical separation of contaminants) or wet (e.g. wash out         with water) cleaning steps. Dependent on the cleaning procedure         this step may additionally include a drying step. This could be         done e.g. in an air flow.     -   b. Crushing the carob fruits: this could be done, e.g. by         passing the carob fruit through a mill, typically a hammer mill,         to shred the pods to pieces smaller than 3 cm.     -   c. Separation of carob seeds and kibbled carob pulp: the seed         can be separated using a sieve with a suitably sized mesh,         depending on the conditions of the process, the agronomical         variety and the water contents of the fruit. As an alternative         suitable process air classification or other mechanical or         physical technologies can be used.     -   d. Toasting (modification of the structure of condensed         tannins): this process is important to change the nutritional         properties of the condensed tannins. This can be reached by         toasting of the carob kibbles at temperatures usually between         130-200° C., typically between 140-150° C. for a certain time         period depending on the water content of the pulp and the         particle size. Usual time periods for this toasting process are         5-60 minutes, typically 10-20 minutes.     -   e. Extraction process: the toasted carob pulp is extracted with         water or any other suitable solvent to remove the sugars and         water-soluble tannins. The ratio of extraction material to         solvent is usually higher than 1:20 (by weight), typically 1:4         (by weight). The extraction can be made at different         temperatures usually in the range of 5-80° C., typically between         20-55° C. Extraction can be done e.g. in an simple extraction         tank (with or without stirrer) or in a continuously operating         extractor (counter current flow extraction). Dependent on the         other extraction parameters extraction time usually lies between         5 minutes to 24 hours, typically between 15 minutes and 2 hours.     -   f. Separation: Separation of the water soluble components from         the water insoluble parts can be done by several techniques         including decantation, filtration, or centrifugation.     -   g. Milling: the water-insoluble residue is ground to a fine         powder by milling techniques. Preferred equipment is a colloidal         mill, but also other milling techniques can be considered (e.g.         ball mills). Reached particle sizes are below 250 μm (90% of         particles below 250 μm), usually below 150 μm (90% of particles         below 150 μm) and typically below 100 μm (90% of particles below         100 μm).     -   h. Optionally repetition of steps e. (extraction) and f.         (separation) to further reduce the water soluble constituents in         the obtained residue. Two further extraction steps are         sufficient to reach sugar contents usually below 15% and         typically below 10% in the insoluble residue.     -   i. Separation: After the last extraction step the obtained         residue is pressed, filtered, decanted, or centrifuged to         eliminate as much as possible of the water.     -   j. Drying: To reduce the water content usually below 8%,         typically below 6%. This can be managed by several drying         techniques including a drying oven, spray drying, vacuum drying,         drying in an air or inert gas stream. Temperatures should         usually not lie above 140° C., typically not above 60-65° C.     -   k. Classification (sieving): dependent on the application the         obtained product can be sieved to obtain standardized particle         size limits.

The whole production process, as described above in the steps a-k, or parts of it, can also be done in a continuous way.

The properties of this denatured carob flour: hypocholesterolemiant, regulator of gastrointestinal dynamics, bile salt chelant and antioxidant on which we base its potential dietary and pharmacological applications for both human and animals, have been demonstrated in a number of animal trials carried out in the Department of Nutrition of the Universidad Complutense de Madrid, of which we summarize some relevant results.

First of all, in experimental animals the influence of this denatured carob flour (DCF) on ingestion, weight increase, growth, fecal volume, fecal polyphenol and butyrates was studied. To do this, a total of three batches of 10 growing rats were fed isocaloric synthetic diets modified to suit their nutritional requirements in which the only variable was the type of dietary fiber used: 2% apple pectin in all batches as butyrate source and 5% in batch 1 of microcrystalline cellulose (Avicel R), 5% in batch 2 of carob fiber (NCF=Natural Carob Fibre) and 5% in batch 3 of DCF. It was found that intake of DCF did not affect weight increase in animals or the dietary efficacy of the diets compared to cellulose and it can, therefore, be concluded that the treatment has managed to eliminate the antinutritive effect of its condensed tannins, while the carob fiber (NCF), slightly but significantly reduces both parameters. The DCF increases fecal volume and weight compared to cellulose and results in a similar fecal volume and weight, at the same doses, as NCF, but with fecal butyrate and polyphenol concentrations 30% and 10% higher, respectively, in rats fed with our invention than in those fed with diets containing carob fiber (NCF), hence, as repeatedly described by several authors, protection against the formation of mutagenic or carcinogenic compounds (electrophylic molecules) in animals that consume DCF is higher than that achieved with carob fibers (NCF).

To determine its effects on blood lipids, 30 young rats with experimental hypercholesterolemia were used (total cholesterol 235 mg/dl), 5 groups with 10 rats each were formed and the following fiber sources were added to their diets:

Batch 1-10% cellulose

Batch 2-10% carob fiber (NCF)

Batch 3-10% carob flour (DCF)

After three weeks of treatment mean serum cholesterol levels were:

Batch 1: 285 mg/dl

Batch 2: 165 mg/dl

Batch 3-112 mg/dl

The conclusions of this study can be summarized as follows:

Taking into account that the cellulose used had no effect on cholesterolemia and that our invention (DCF) produced, significantly (p<0.05), the greatest reduction in serum cholesterol levels in animals, we can conclude that our invention has a more pronounced effect on cholesterolemia than natural carob fibers (NCF). This effect seems to be mediated by more sequestration of bile salts by DCF.

The percentages, temperatures and other additional factors associated with the product and with the process described can be variable provided that they are additional and secondary and do not alter the essence of the patent described here. 

1. Denatured carob flour comprising 2-15% sugars, 0.2-1.5% cyclitols (pinitol), 2-10% lignins, 10-30% celluloses, 3-20% hemicelluloses, 1-6% pectins, 25-55% condensed tannins, 3-9% protein and less than 8% water.
 2. Denatured carob flour according. to claim 1, wherein the sugar content is 3-10%.
 3. Denatured carob flour according to claim 1, wherein the cyclitols content is 0.3-1%.
 4. Denatured carob flour according to of claim 1, wherein the lignins content is 2-7%. one
 5. Denatured carob flour according to of claim 1, wherein the celluloses content is 15-28%.
 6. Denatured carob flour according to claim 1, wherein the hemicelluloses content is 3-9%.
 7. Denatured carob flour according to claim 1, wherein the pectins content is 2-5%.
 8. Denatured carob flour according to claim 1, wherein the condensed tannions content is 30-48%.
 9. Denatured carob flour according to claim 1, wherein the protein content is 4-8%.
 10. Denatured carob flour according to claim 1, wherein the water content is less than 6%.
 11. Process to obtain a flour according to claim 1, comprising the following steps: a. cleaning the whole fruit; b. crushing the carob fruits; c. separating carob seeds and kibbled carob pulp; d. toasting between 130-200° C.; e. extracting; f. separating; g. milling 90% of particles below 250 μm; h. separating: i. drying below 8% and j. classifying (sieving).
 12. Process according to claim 11, wherein in step b. the carob pod is shredded into pieces smaller than 3 cm.
 13. Process according to claim 11, wherein the temperature is between 140-150° C.
 14. Process according to claim 11, wherein the time period for the toasting process is 5-60 minutes.
 15. Process according to claim 14, wherein the time period is 10-20 minutes.
 16. Process according to claim 11, wherein in step e. the extraction is performed in the range of 5-80° C.
 17. Process according to claim 11, wherein in step e. the ratio of pulp to water is 1:20 (wt./wt.).
 18. Process according to claim 11, wherein in step e. the extraction is performed for 5 minutes to 24 hours.
 19. Process according to claim 11, wherein in step g. 90% of particles are below 150 μm.
 20. Process according to claim 11, wherein between steps g. and h. steps e. and f. are at least once repeated.
 21. Process according to claim 11, wherein in step i. the drying is performed at a temperature which does not exceed 140° C.
 22. Process according to claim 11, wherein the process is carried out continuously.
 23. Foods, dietary supplements, animal feed, pet food, human or animal medicine comprising flour according to claim
 1. 